Our Services

Strategic advisory

Vergio offers strategic advisory services regarding drug development , drug candidates registration and market access in European Union.

Clinical development

We provide services to help life science and biopharmaceutical clients to design the clinical development of their drug candidates taking into account clinical and non-clinical data, regulatory and market access requirements, and operational/financial constraints.
We offer medical writing and scientific articles preparation for the publication of your clinical study results.

Statistical analyses

We conduct review/audit of statistical analyses.
To improve efficiency of the clinical trial design, we perform statistical simulations to explore the effect of key trials parameters and multiple scenarios.
We further analyse clinical trials results to better characterize drug efficacy and safety profile.

Registration

We help life science and biopharmaceutical clients to define the registration strategy, to prepare the pre-submission steps (scientific advice, orphan drug designation procedure, pre-submission meetings, registration dossier preparation), and to support the registration process for centralized, decentralized and national procedures in the European Union.

Market access

We conduct research work to further support drug efficacy, safety and benefit-risk such as (network) meta-analysis, systematic literature review.

Due diligence

We offer business plan preparation services and we conduct audits of clinical data or development program for due-diligence purposes.